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Medical Device Risk Management Jobs in Arizona (NOW HIRING)

Intellectt INC

Senior medical device risk management experience -- 7-10+ yrs preferred * Deep expertise in ISO 14971 and FDA QMSR risk management requirements * Experience building or remediating complete risk ...

Intellectt INC

Design Transfer Risk SME

Yuma, AZ · On-site

Medical device risk management experience with focus on design transfer * Familiarity with ISO 14971 and QMSR risk expectations * Experience reviewing design transfer documentation with risk ...

Beltone

Medical Device Sales

Prescott, AZ · On-site

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... Cash Management procedures are executed. • Track and provide feedback on all referrals from ...

Beltone

Medical Device Sales

Prescott, AZ

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... Manage assigned office, including supervision of Patient Care Coordinator Maintain a clean work ...

Gn

Medical Device Sales

Prescott, AZ

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... Manage assigned office, including supervision of Patient Care Coordinator Maintain a clean work ...

(unknown company)

Director Risk Management

Tucson, AZ · On-site

Comprehensive Health Coverage - Medical, dental, and vision plans to keep you and your family ... Directs and manages the facility's risk management program, identifying and evaluating risks ...

Aptyx

Quality Manager- MED DEVICE ISO13485

Tempe, AZ · On-site

Ensure all Device History Records (DHRs), Device Master Records (DMRs), and validation ... Provide quality input into production planning, risk management, and decision-making * Candidates ...

American Express

Manager - Risk Management

Phoenix, AZ · On-site

Fraud Risk colleagues are industry's most innovative thinkers and creative problem solvers with ... Comprehensive medical, dental, vision, life insurance, and disability benefits * Flexible working ...

American Express

Manager - Risk Management

Phoenix, AZ · On-site

$89K - $150K/yr

Fraud Risk colleagues are industry's most innovative thinkers and creative problem solvers with ... Comprehensive medical, dental, vision, life insurance, and disability benefits * Flexible working ...

LivaNova

Manager, Enterprise Risk Management

Phoenix, AZ

$110K - $150K/yr

... Enterprise Risk Management is responsible for overseeing and coordinating the organization ... Health benefits - Medical, Dental, Vision * Personal and Vacation Time * Retirement & Savings Plan ...

NexGoal

Medical Device Sales Representative

Phoenix, AZ · On-site

Build and maintain positive working relationships with medical and administrative support staff ... Track all communication through a CRM system. * Review quality control of processes. Qualifications

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All JobsMedical Device Risk Management JobsMedical Device Risk Management Jobs in Arizona

Medical Device Risk Management information

See Arizona salary details

$48K

$104K

$158.4K

How much do medical device risk management jobs pay per year?

As of Jun 13, 2026, the average yearly pay for medical device risk management in Arizona is $103,958.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,900.00 and $120,200.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Medical Device Risk Management, and why are they important?

To thrive in Medical Device Risk Management, you need a solid background in engineering or life sciences, a thorough understanding of regulatory standards (such as ISO 14971), and experience in risk assessment processes. Familiarity with risk management software, quality management systems, and relevant regulatory databases is typically required, along with certifications like Certified Risk Manager (CRM) or RAC. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for evaluating risks and collaborating with cross-functional teams. These competencies ensure the safety and compliance of medical devices, protecting both end-users and the company from regulatory or safety issues.

What is the difference between Medical Device Risk Management vs Medical Device Quality Assurance?

AspectMedical Device Risk ManagementMedical Device Quality Assurance
Primary FocusIdentifying, evaluating, and mitigating risks associated with medical devicesEnsuring products meet quality standards and regulatory requirements
CertificationsISO 14971, RAPS certifications often preferredISO 13485, regulatory compliance certifications
Work EnvironmentDesign and development teams, risk analysis meetingsManufacturing, inspection, and quality control departments
Industry UsageUsed throughout product lifecycle for safety managementUsed to maintain product quality and compliance

While both roles are essential in the medical device industry, Risk Management focuses on minimizing safety risks throughout the product lifecycle, whereas Quality Assurance ensures products consistently meet quality and regulatory standards. Understanding these differences helps professionals align their skills with industry needs.

What is medical device risk management?

Medical device risk management is the systematic process of identifying, evaluating, and controlling risks associated with medical devices throughout their lifecycle. This process ensures that potential hazards are minimized to protect patient safety and comply with regulatory standards, such as ISO 14971. Risk management includes activities like risk assessment, implementing controls, monitoring, and documenting all steps to demonstrate compliance. It is a critical function in the design, manufacturing, and post-market phases of medical device development.

How does a Medical Device Risk Management professional typically collaborate with cross-functional teams during the product development lifecycle?

Medical Device Risk Management professionals work closely with engineering, regulatory affairs, quality assurance, and clinical teams to identify, assess, and mitigate potential risks associated with medical devices. They participate in design reviews, facilitate risk assessments such as FMEA, and ensure that risk controls are effectively implemented and documented according to regulatory standards like ISO 14971. Regular communication and collaboration are essential to align risk management activities with project timelines and compliance requirements, ensuring patient safety and product success.
What are popular job titles related to Medical Device Risk Management jobs in Arizona? For Medical Device Risk Management jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Medical Device Risk Management jobs in Arizona look for? The top searched job categories for Medical Device Risk Management jobs in Arizona are:
What cities in Arizona are hiring for Medical Device Risk Management jobs? Cities in Arizona with the most Medical Device Risk Management job openings:
Medical Device Risk Management jobs near you
Risk Management File SME

Risk Management File SME

Intellectt INC

On-site

Contractor

Posted 14 days ago

Job description

Hello,

I hope you’re doing well.

My name is Vyshu, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Risk Management File SME based in Remote (EST) with one of our prestigious clients.
I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at vyshnavi.t@intellectt.com

Role: Risk Management File SME
Location: Remote EST

Summary:
Senior level (7–10+ yrs). Focuses specifically on assessing and remediating the overall Risk Management File. Must have deep experience building and maintaining complete risk management files for complex medical devices.

Key Responsibilities

  • Assess and remediate the overall Risk Management File for the device
  • Ensure the risk management file is complete, consistent, and compliant with ISO 14971
  • Identify and close gaps in risk documentation across all phases
  • Integrate risk outputs from all workstreams into a cohesive risk management file
  • Collaborate with Risk COE and all workstream leads

Required Qualifications

  • Senior medical device risk management experience — 7–10+ yrs preferred
  • Deep expertise in ISO 14971 and FDA QMSR risk management requirements
  • Experience building or remediating complete risk management files
  • Experience across multiple design control phases with risk integration
  • Experience in remediation initiatives in regulated environments

Thanks & Regards,
Vyshnavi Thuraka
Recruiter
Intellectt Inc 
vyshnavi.t@intellectt.com
Direct: 732 204 6550
Desk number: 732 412 6999 - Ext: 225